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Prognostic significance of UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-3 (GalNAc-T3) expression in patients with gastric carcinoma
Authors:Onitsuka Koji  Shibao Kazunori  Nakayama Yoshifumi  Minagawa Noritaka  Hirata Keiji  Izumi Hiroto  Matsuo Ken-ichi  Nagata Naoki  Kitazato Kenji  Kohno Kimitoshi  Itoh Hideaki
Affiliation:Departments of Surgery 1;Molecular Biology, University of Occupational and Environmental Health School of Medicine, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807–8555;Hanno Research Center, Taiho Pharmaceutical Co., Ltd., 1–27 Misugidai, Hanno, Saitama 357–8527
Abstract:Aberrant glycosylation occurs during development of gastric carcinomas. The initiation of mucin-type O -glycosylation is regulated by GalNAc-T3 (UDP- N -acetylgalactosamine:polypeptide N -acetyl-galactosaminyltransferase-3). However, the clinical significance of GalNAc-T3 expression in human gastric carcinoma has not yet been demonstrated. In the present study, we investigated the relationship between immunohistochemical GalNAc-T3 expression and various clinicopathologic factors, including prognosis, in 117 gastric carcinoma patients. Of 117 gastric carcinomas examined, 59 (50.4%) showed strong expression of GalNAc-T3. Strong expression was detected in 38 of 59 (64.4%) differentiated type and in 21 of 58 (36.2%) undifferentiated gastric carcinomas, indicating that the expression of GalNAc-T3 correlated significantly with tumor differentiation (P=0.0023, x 2 test). Overall 5-year survival rate in patients with strong GalNAc-T3 expression (71.0%) was significantly better than that of patients with weak expression (49.3%) (P=0.0197, log-rank test). Multivariate analysis identified GalNAc-T3 expression as an independent prognostic factor ( P =0.0158, Cox proportional hazards model). Our data suggest that GalNAc-T3 expression may be a useful marker for prognosis and differentiation of gastric carcinomas. (Cancer Sci 2003; 94: 32 – 36)
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